Year 5 Core Conditions > Cardiovascular - Level 3 > Flashcards

Cardiovascular - Level 3 Flashcards

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1
Q

Definition of accelerated hypertension?

A
  • Severe increase in blood pressure to 180/120 mmHg or higher with signs of retinal haemorrhage and/or papilledema (swelling of the optic nerve);
  • Also known as malignant hypertension
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2
Q

Epidemiology of accelerated hypertension?

A
  • Average age is 40 years
  • Men more commonly
  • Black ethnicity
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3
Q

Causes of accelerated hypertension?

A 
o	Renovascular disease – renal artery stenosis
o	Renin-secreting neoplasms
o	Renal vasculitis – scleroderma, polyarteritis, SLE
o	Phaeochromocytoma
o	Cocaine abuse
o	MAOIs, COCP
o	Glomerulonephritis
o	Pre-eclampsia/Eclampsia
o	Hyperthyroidism/Hypothyroidism
o	Cushing’s syndrome
o	Acromegaly
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4
Q

Symptoms of accelerated hypertension?

A
  • May be asymptomatic
  • Symptoms
    o Headache
    o Fits
    o N&V
    o Visual disturbances
    o Chest pain
    o Neurological changes
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5
Q

Initial investigations to perform in accelerated hypertension?

A
  • Blood pressure – lying and standing and in both arms
  • Fundoscopy
  • Bloods
    o FBC, clotting, U&E, LFTs, TFTs, glucose, troponin
  • Urine dipstick
  • CXR – cardiac size, cardiac failure
  • ECG – LVH
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6
Q

Investigations to find cause of accelerated hypertension?

A 
o	CT/MRI of head/kidneys
o	Plasma renin
o	Plasma aldosterone
o	24-hour urine VMA and metanephrin levels
o	ANA
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7
Q

Referral in people with accelerated hypertension?

A
  • Refer for same-day specialist assessment if >180/120 and:
    o Signs of retinal haemorrhage or papilloedema OR
    o Signs of new onset confusion, CP, HF, AKI
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8
Q

Management of accelerated hypertension?

A
  • Reduce BP over 24-48 hours
    o IV labetalol (alternatives nitroprusside /nicardipine)
     Every 10 minutes according to response
    o If LV failure – IV furosemide, GTN and nifedipine
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9
Q

Definition of pericarditis?

A
  • Acute inflammation of pericardium (membranous sac surrounding heart) and can co-exist with myocarditis
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10
Q

PAthology of pericarditis?

A

o Pericardial vascularisation and infiltration with leukocytes
o Exudate and adhesion within pericardial sac and serous effusion

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11
Q

Epidemiology of pericarditis?

A

o 5% of ED visits with chest pain
o Usually post-viral or idiopathic
o Can become recurrent if >1 episode

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12
Q

Causes of pericarditis?

A

o Myocardial infarction (including Dressler’s syndrome)
o Viral - Coxsackie, Echovirus, EBV
o Bacterial - Pneumococcus, meningococcus, haemophilus, staphylococcus, TB
o Neoplasms, Uraemia, SLE, rheumatoid arthritis
o Drug - Hydralazine, procainamide

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13
Q

Symptoms of pericarditis?

A

o Chest pain
 Sharp, central or retrosternal
 Radiates to neck, trapezius ridge or shoulders
 Worse on deep inspiration, exercise, swallowing and lying flat
 Relieved by sitting up and leaning forward
o May have cough, chills, weakness

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14
Q

Signs of pericarditis?

A

Pericardial friction rub
 Often intermittent, positional and elusive
 Louder during inspiration and may be heard on systole and diastole
 Scratchy superficial sound, loudest in midline and lower left parasternal edge
Low grade fever
Tachycardia
Tachypnoea

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15
Q

Investigations of pericarditis?

A

ECG
o Concave-upward ST segment elevation
o PR depression in limb and pre-cordial leads
o Reciprocal PR elevation and ST depression in aVR

CXR
o Flask-shaped cardiac silhouette sign of large pericardial effusion

Bloods
o FBC, U&Es, CRP, ESR and troponin

Blood cultures if evidence of sepsis

Echocardiogram
o If pericardia effusion or cardiac tamponade suspected

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16
Q

Management of pericarditis?

A

o Benign or self-limiting
o Rest
o High dose NSAIDs (naproxen 250mg TDS/QDS) +/- PPI cover
 Give 7-14 days then taper off

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17
Q

Management of pericardial effusion in pericarditis?

A

o Senior help, immediate echocardiogram

o Pericardiocentesis under US and then drainage or open thoracotomy

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18
Q

Management of constrictive pericarditis in pericarditis?

A

o Pericardial resection

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19
Q

Prognosis of pericarditis?

A
  • Most improve over days to weeks

- Recurrence in around 1 in 3 patients

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20
Q

Definition of pericardial effusion?

A
  • Accumulation of fluid in pericardial sac
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21
Q

Causes of pericardial effusion?

A

o Viruses (Coxsackie, flu, EBV, mumps, varicella, HIV)
o Bacteria (pneumonia, rheumatic fever, TB, staphs)
o Fungi
o MI and Dressler’s syndrome
o Drugs – Procainamide, hydralazine, penicillin
o Others – uraemia, RA, SLE, trauma, surgery, malignancy

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22
Q

Symptoms of pericardial effusion?

A

o SOB
o Symptoms of pericarditis – sharp chest pain, radiating to scapular ridge, relieved by sitting up and worsening with inspiration
o Syncope
o Cough

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23
Q

Signs of pericardial effusion?

A

o Raised JVP (prominent X descent)
o Bronchial breathing at left base (Ewart’s sign)
o Look for signs of cardiac tamponade
 Tachycardia, pulsus paradoxus, hypotension, raised JVP, muffled S1 and S2

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24
Q

Investigations of pericardial effusion?

A
  • Bloods
    o FBC, U&Es, CRP, cardiac enzymes
    o Blood cultures if needed
  • CXR
    o Enlarged, globular heart
  • ECG
    o Low voltage QRS complexes and alternating QRS morphologies
  • Echocardiogram
    o Echo-free zone surrounding heart
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25
Management of pericardial effusion?
- Treat cause - Oxygen if needed - Pericardiocentesis o Therapeutic in cardiac tamponade o Pericardial fluid sent for culture, ZN stain/TB culture and cytology
26
Complications of pericardial effusion?
o Pericardial tamponade | o Chronic pericardial effusion
27
Definition of cardiomyopathy?
myocardial disorder in which myocardium is structurally or functionally abnormal without coronary artery disease, hypertension, valvular or congenital heart disease
28
Causes of cardiomyopathy?
o Primary – idiopathic and not attributed to a cause o Secondary – associated with:  CKD, cirrhosis, obesity, stress  SLE/sarcoidosis/amyloidosis  Diabetes, thyroid, acromegaly, haemochromatosis  Cocaine, alcohol, chemotherapy  Trypanosomiasis, viruses  Malnutrition, deficient Vit B, calcium, magnesium  Hypertension, IHD, valvular disease  Duchenne  Peripartum cardiomyopathy – between last month and 5-6 months after delivery
29
Definition of dilated cardiomyopathy?
o Ventricular chamber enlargement and contractile dysfunction with normal LV wall thickness o RV may be dilated and dysfunctional too
30
Epidemiology of dilated cardiomyopathy?
- Most frequent indication for heart transplant - Prevalence – 0.2% - More common in males
31
Associations of dilated cardiomyopathy?
``` o Ischaemia o Genetic (Barth syndrome) o Alcohol o Thyrotoxicosis o RA, SLE o Drugs – cocaine, amphetamines, heroin o Peri/Post-partum o Haemochromatosis, sarcoidosis, amyloidosis o Virus – adenovirus, CMV, coxsackie, Lyme, toxoplasmosis ```
32
Symptoms of dilated cardiomyopathy?
o Asymptomatic o Heart failure symptoms – exertional SOB, orthopnoea, PND, weakness, fatigue, oedema o AF
33
Signs of dilated cardiomyopathy?
``` o Tachycardia o AF o Low BP o Raised JVP o Displaced, diffuse apex beat o Loud 3rd and/or 4th HS o Mitral/Tricuspid regurgitation o Signs of heart failure – pleural effusion, oedema, hepatomegaly, ascites ```
34
Investigations of dilated cardiomyopathy?
- ECG o Tachycardia, non-specific T wave changes, LBBB - Bloods o FBC, U&E, LFT, TFTs, BNP, troponins - CXR o Cardiomegaly, pulmonary oedema - Echocardiogram o Globally dilated hypokinetic heart with low EF, may have MR/TR, LV mural thrombus
35
Diagnostic investigations of dilated cardiomyopathy?
- Cardiac Catheterisation - Cardiac MRI - Endomyocardial biopsy
36
Investigations to find cause of dilated cardiomyopathy?
o Genetics, serologies, electrophysiology, exercise testing, iron levels, vitamin levels, ANA
37
Management of dilated cardiomyopathy - pharmacological management?
- Bed rest o Diuretics  Furosemide - if symptomatic with fluid overload  Spironolactone if low K with furosemide o ACEi o Beta-blockers o Digoxin  Inadequate response to ACE inhibitors and diuretics if AF or tachycardia
38
Management of dilated cardiomyopathy - surgical management?
- Pacing Support o Biventricular pacing (CRT)  If NYHA class 3 or 4 with QRS prolongation  With ICD - Surgical o Heart transplant  80% one-year survival o LV assist devices
39
Complications of dilated cardiomyopathy?
o Progressive heart failure | o Sudden cardiac death
40
Definition of hypertrophic cardiomyopathy?
o Autosomal dominant genetic disorder o Disorganised cardiac myocytes due to mutations in genes of sarcomeric proteins (cardiac B-myosin, troponin, A-tropomyosin) o LV hypertrophy, impaired diastolic filling and abnormalities of mitral valve o Can cause obstruction of LVOT (HOCM), diastolic dysfunction, myocardial ischaemia and risk of tachyarrhythmias
41
Epidemiology of hypertrophic cardiomyopathy?
- Most common CV genetic disease - Prevalence 0.2% - Men, 20-30 years old, Black people - Most common cause of SCD in young people and athletes
42
Symptoms of hypertrophic cardiomyopathy?
- Mostly asymptomatic o SOB, chest pain, palpitations, syncope o Sudden death – due to arrhythmias or obstruction of LVOT
43
Signs of hypertrophic cardiomyopathy?
o Forceful apex beat  Double impulse if LVOT obstructed o Late ejection systolic murmur (augmented by standings or Valsalva)  Left sternal edge, radiating to aortic and mitral areas o JVP ‘a’ wave prominent o AF o BP changes during upright exercise
44
ECG findings in hypertrophic cardiomyopathy?
o LVH o Deep, narrow (“dagger-like”) Q waves in the lateral (V5-6, I, aVL) and inferior (II, III, aVF) leads o T-wave inversion o AF, VT
45
Echo findings in hypertrophic cardiomyopathy?
o Asymmetrical septal hypertrophy (>15mm) with ratio of septal to posterior of >1.4:1 o Small LV cavity o Hypercontractile posterior wall o Mid-systolic closure of aortic valve o Systolic anterior motion of mitral valve
46
CXR findings in hypertrophic cardiomyopathy?
o Heart size normal or enlarged | o LA enlargement seen
47
Further testing needed in hypertrophic cardiomyopathy?
o Exercise ECG + Holter monitor  Risk stratification – increased if blunted systolic BP to exercise, ventricular arrhythmias, progressive ST depression and symptoms o Nuclear tests and cardiac catheterisation o Cardiac MRI  If poor visualisation on Echo
48
Screening in hypertrophic cardiomyopathy?
o Echocardiogram  First-degree family members of affected patients • Repeat every 12-24 months throughout adolescence o ECG  Athletes
49
Management of asymptomatic hypertrophic cardiomyopathy?
 ICD • If 1st degree relative with SCD, LV wall thickness >30mm, unexplained syncope  Restrict from high-intensity athletics
50
Management of symptomatic hypertrophic cardiomyopathy - drug management?
``` • Beta-blockers (atenolol) • Verapamil • Disopyramide o To reduce LVOT gradient and diastolic dysfunction • Amiodarone o To suppress arrhythmias • Anticoagulation – NOAC/Warfarin ```
51
Management of symptomatic hypertrophic cardiomyopathy - surgical?
 Surgical • Catheter ablation for AF if drug refractory • Septal myomectomy (surgical or alcohol ablation) o If refractory symptoms or elevated resting outflow gradients • Heart Transplant if refractile  Pacing • ICD implantation if risk factors
52
Prognosis of hypertrophic cardiomyopathy?
o Variable – can remain asymptomatic or progress with heart failure o Competitive sport increases risk of sudden death
53
Definition of restrictive cardiomyopathy?
o Normal LV cavity size and systolic function but increased myocardial stiffness o Ventricle incompliant and fills predominantly in early diastole o Associated with raised LA pressure, atrial dilatation
54
Epidemiology of restrictive cardiomyopathy?
- Least common cardiomyopathy - 5% of all cardiomyopathies - Elderly - Tropical Africans
55
Causes of restrictive cardiomyopathy?
``` o Idiopathic o Loffler’s syndrome (endomyocardial fibrosis) o Infiltrative myocardial disease o Amyloidosis (MC in West) o Sarcoidosis o Haemochromatosis o Fabry’s disease ```
56
Symptoms of restrictive cardiomyopathy?
o Heart Failure – SOB, fatigue, oedema | o Similar to constrictive pericarditis
57
Signs of restrictive cardiomyopathy?
``` o Loud 3rd HS o RVF predominate  Raised JVP (prominent x and y descents)  Hepatomegaly  Oedema  Ascites o AF ```
58
Investigations and findings of restrictive cardiomyopathy?
- ECG o Tachycardia, non-specific T wave changes, LBBB - Bloods o FBC, U&E, LFT, TFTs, BNP, troponins - CXR o Cardiomegaly, pulmonary oedema - Echocardiogram o Thickened ventricular walls, valves and atrial septum with small cavities
59
Diagnostic imaging in restrictive cardiomyopathy?
- Cardiac Catheterisation - Cardiac MRI – distinguish restrictive CM and constrictive pericarditis - Cardiac biopsy
60
Management of restrictive cardiomyopathy?
- Treat cause - Management of Heart Failure o Diuretics  Furosemide  Spironolactone o ACEi ``` - Other managements o Amiodarone o Anticoagulation if AF – NOACs/Warfarin o Pacemakers/ICD o Transplantation ```
61
Definition of arrhythmogenic right ventricular cardiomyopathy?
o Fibro-fatty replacement of RV myocytes due to apoptosis, inflammation or genetics
62
Epidemiology of ARVC?
- Prevalence – 1 in 2000 - Presents in adolescence or early childhood - Males - Autosomal dominant (more common), also recessive - Common cause of SCD in young people
63
Symptoms of ARVC?
- Men aged 15-35 o Palpitations o Presyncope o Syncope o SCD
64
Signs of ARVC?
o Atrial arrhythmias
65
Phases of ARVC?
o Concealed – subtle RV changes, minor arrhythmias – asymptomatic or SCD o Overt electrical disorder – symptomatic RV arrhythmias with abnormal RV wall – palpitations and syncope – arrhythmias and SCD common o RV failure – extension of disease to whole RV causes dysfunction o Biventricular pump failure – LV involved leads to HF
66
Investigations of ARVC?
``` - ECG o Ventricular arrhythmias, LBBB - Bloods o FBC, U&E, LFT, TFTs, BNP, troponins - CXR - Echocardiogram ```
67
Diagnostic imaging of ARVC?
- Cardiac Catheterisation - Cardiac MRI o RV enlargement, fatty infiltration, fibrosis and wall motion abnormalities - Cardiac biopsy
68
Management of non-threatening ventricular arrhythmias?
o Beta-blockers (sotalol) | o Amiodarone
69
Management of sustained VT/VF?
o Serial therapeutic drug trials using programmed ventricular stimulation o ICD  If inducible or present with syncope/cardiac arrest o Radio-frequency ablation (if localised disease)
70
Prognosis of ARVC?
o Progressive deterioration of RV function | o Mortality rate 1-3% per year
71
Pathology of aortic dissection?
o Longitudinal splitting of muscular aortic media by column of blood o Dissection may spread proximally, distally, rupture internally back into aortic lumen or externally Lead to: o Aortic incompetence, coronary artery blockage, cardiac tamponade o Rapid exsanguination
72
Classification of aortic dissection?
o Stanford Type A (70%)  Ascending aorta involved o Stanford Type B (30%)  Ascending aorta not involved
73
Risk factors of aortic dissection?
``` o Hypertension (70%) o Bicuspid aortic valve o Marfan’s syndrome o Ehlers-Danlos syndrome o Recent cardiac surgery or angiography/angioplasty ```
74
Symptoms of aortic dissection?
o Abrupt onset sharp, tearing or ripping pain (maximal at onset) in anterior and posterior chest o Syncope o Hemiplegia (occlusion of carotid artery) o Anuria (occlusion of renal arteries) o Paraplegia (occlusion of spinal artery)
75
Signs of aortic dissection?
o Aortic regurgitation murmur (30%) o Asymmetrical peripheral pulses or pulse deficit o Hypertension o Hypotension – features of tamponade or neurological signs
76
Investigations of aortic dissection?
``` - Bloods o FBC, U&E, coagulation, glucose and cross-matching - ECG o MI, LVH, ischaemia - CXR o Widened mediastinum o Double knuckle aorta o Deviation of trachea o Calcium sign – separation of two parts of wall of calcified aorta - CT Angiography o Definitive diagnosis ```
77
Management of aortic dissection?
o High flow O2 using face mask o Insert 2 wide-bore IV cannulas and cross-match 10U of blood (inform blood bank of suspected diagnosis) o IV morphine + Antiemetic o Call cardiothoracic team and cardiologist early  All Type A dissections treated surgically  Type B managed medically or surgically (if leaking, ruptured, compromising vital organs) o Insert arterial line (right radial artery) and discuss how to control BP (Aim 100-110mmHh using labetalol infusion)
78
Epidemiology of acute mesenteric ischaemia?
o >50 years old | o Mostly small bowel
79
Causes of acute mesenteric ischaemia?
Arterial (thrombotic, embolic)  AF, MI, mitral stenosis, endocarditis, arterial catheterisation  Atherosclerosis, aortic aneurysm, heart failure, dehydration Non-occlusive (low-flow states – poor cardiac output)  Hypotension, cocaine, digitalis Venous thrombosis  Hypercoagulability (protein C and S deficiency, tumours, infection) Trauma, Vasculitis, Radiotherapy
80
Symptoms of acute mesenteric ischaemia?
 Acute severe abdominal pain • Constant, central or around RIF  No abdominal signs  Rapid hypovolaemia – then shock
81
Investigations of acute mesenteric ischaemia?
``` o Bloods  Raised Hb, WCC, amylase  Metabolic acidosis o AXR o CT angiography – gold standard o MR oximetric measurement of superior mesenteric vein flow ```
82
Medical management of acute mesenteric ischaemia?
 Fluid resuscitation  NG tube  IV gentamicin + metronidazole  IV UFH
83
Surgical management of acute mesenteric ischaemia?
 Prompt laparotomy if peritonitis  Arteriography and thrombolytics/Revascularisation  Resection of dead bowel
84
Prognosis of acute mesenteric ischaemia?
o Poor – mortality 50-90% in arterial and non-occlusive disease
85
Complications of acute mesenteric ischaemia?
o Septic peritonitis | o SIRS into multi-organ dysfunction syndrome
86
Definition of chronic mesenteric ischaemia?
- Chronic atherosclerotic disease of vessels supplying intestine - Known as intestinal angina – usually all three major mesenteric arteries involved
87
Epidemiology of chronic mesenteric ischaemia?
o Low incidence – mainly females 50-70 tears old
88
Risk factors of chronic mesenteric ischaemia?
o Hx of CVD | o Smoking, hypertension, diabetes, hyperlipidaemia
89
Symptoms of chronic mesenteric ischaemia?
``` o Abdominal Pain  Moderate-to-severe colicky or constant pain  Often post-prandial o Eating hurts o Weight loss and fear of eating ```
90
Signs of chronic mesenteric ischaemia?
o Vague abdominal tenderness o Abdominal bruit o PR bleeding o N&V
91
Investigations of chronic mesenteric ischaemia?
o Bloods – FBC, LFT, U&Es – dehydration and malnutrition o CXR o ECG o CT angiography – gold standard
92
Management of chronic mesenteric ischaemia - asymptomatic?
 Smoking cessation and antiplatelet therapy
93
Management of chronic mesenteric ischaemia - symptomatic?
 Surgery- Percutaneous transluminal angioplasty and stent insertion (option for open)  May need TPN
94
Definition of ischaemic colitis?
- Compromised blood circulation supplying the colon
95
Epidemiology of ischaemic colitis?
o Disease of the elderly mostly – average age 70
96
Risk factors of ischaemic colitis?
o Thrombosis – IMA thrombosis o Emboli – mesenteric arterial emboli, cholesterol emboli o Decreased CO o Shock o Trauma o Strangulation o Drugs – digitalis, oestrogens, antihypertensives, cocaine, COCP o Surgery – cardiac bypass, aortic dissection repair o Vasculitis – SLE, polyarteritis nodosa, SCC o Hypercoagulability – Protein C&S deficiency, PNH, antithrombin 3 deficiency o Long-distance running
97
Symptoms of ischaemic colitis?
o Acute onset LIF abdominal pain o N&V o Bloody diarrhoea
98
Investigations of ischaemic colitis?
o Colonoscopy and biopsy – gold standard | o Barium enema – thumbprinting of submucosal swelling
99
Management of ischaemic colitis?
o Fluid replacement o Broad-spectrum antibiotics o Surgery – laparotomy and removal of necrotic colon
100
Path of SVC? Definition of SVC obstruction?
- SVC extends from the junction of the right and left innominate veins to the right atrium - SVC provides venous drainage for the head, the neck, the upper extremities and the upper thorax - Caused by extrinsic compression, thrombosis, or invasion of the wall of the superior vena cava - Most commonly by extensive lymphadenopathy in the upper mediastinum (often in patients with lung cancer or lymphoma) - Can occur with any solid tumour (rarer causes include germ cell, breast or oesophageal cancer) - EMERGENCY
101
Epidemiology of SVC obstruction?
- Males > Females | - Malignant causes common when older
102
Aetiology of SVC obstruction - malignant?
```  Lung Cancers  Lymphoma  Mediastinal Lymphadenopathy  Germ cell tumours  Thymoma  Oesophageal ```
103
Aetiology of SVC obstruction - non malignant?
```  Non-malignant tumours  Mediastinal fibrosis  Infection (TB)  Aortic aneurysm  Thrombus ```
104
Symptoms of SVC obstruction?
``` o Headache/“feeling of fullness” in the head o Facial swelling o Dyspnoea (often worse on lying flat) o Cough o Hoarse voice ```
105
Signs of SVC obstruction?
o Facial/upper limb oedema o Prominent blood vessels on the neck, trunk and arms o Cyanosis
106
Investigations of SVC obstruction?
- Chest X-ray | - CT chest
107
Management of SVC obstruction?
- Corticosteroids (dexamethasone 16mg daily) with PPI cover - Urgent vascular stenting - Followed by radiotherapy or chemotherapy depending on primary tumour type - May need LMWH (if thrombus confirmed)
108
Management of SVC obstruction - if cause unknown?
o Bloods: tumour markers o CT chest, abdomen, pelvis o Bronchoscopy/OGD o Biopsy urgently
109
Definition of Raynaud's syndrome?
- Episodic vasospasm that causes digits to change colour to white (pallor) from lack of blood flow - Brought on by cold temperatures - Affected areas subsequently turn blue due to de-oxygenation and/or red perfusion
110
Types of Raynaud's syndrome?
o Primary (idiopathic) RP – no underlying cause o Secondary RP – associated underlying cause (usually connective tissue disorders – scleroderma, systemic lupus erythematosus, rheumatoid arthritis, Sjogren’s syndrome or polymyositis)
111
Epidemiology of Raynaud's syndrome?
- Affects 1-3% of population - Women > Men - Occurs in 20-30s most commonly
112
Causes of secondary Raynaud's syndrome?
``` o Scleroderma  Includes ‘limited cutaneous systemic sclerosis’ – CREST (calcinosis, Raynaud’s phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasia) o SLE o Rheumatoid arthritis o Sjogren’s syndrome o Dermatomyositis and polymyositis o Drugs ```
113
Causes of digital vasospasm - drugs?
```  Amphetamines and cocaine  Beta-blockers  Chemotherapy  Ciclosporin  Interferon-alpha/beta  COCP  Clonidine ```
114
Causes of digital vasospasm - vascular occlusive disease?
 Buerger’s disease  Ateriosclerosis  Thromboembolic disease
115
Causes of digital vasospasm - haematological?
 Polycythaemia  Paraproteinaemia  Leukaemia
116
Causes of digital vasospasm - occupation/environmental?
 Vibration injury  Exposure to vinyl polychloride  Frostbite/Cold injury
117
Causes of digital vasospasm - infections?
 Hep B and C |  Mycoplasma infections
118
Causes of digital vasospasm - endocrine?
 Hypothyroidism  Pheochromocytoma  Carcinoid syndrome
119
Symptoms of Raynaud's syndrome?
o Digits turn white (pallor) then blue with deoxygenation and/or red with reperfusion o Digital pain, paraesthesia
120
Diagnosis of Raynaud's syndrome?
- Clinical Diagnosis | o Diagnose primary Raynaud’s if no features of secondary Raynaud’s present
121
Assessment and testing for secondary Raynaud's syndrome?
- Assess for secondary Raynaud’s o Connective tissue disease  Morning joint stiffness, swollen joints, rash, photosensitivity, hairloss, dry eyes/mouth, FHx o Drugs and Medications - Testing for secondary Raynaud’s o Abnormal nail-fold capillaries (red pen marks, often seen in cuticles) using otoscope, ophthalmoscope or dermatoscope o Digital ulcers o Bloods – FBC, ESR, ANA, creatinine
122
When to suspect secondary Raynaud's syndrome?
``` o Onset >30 years o Episodes intense, painful and asymmetrical o Positive ANA o Abnormal nail beds o Ulcers ```
123
Management of severe ischaemia in Raynaud's syndrome?
Admission
124
Referral to secondary of Raynaud's syndrome?
o All secondary Raynaud’s syndrome | o Children 12 years or less
125
General advice in Raynaud's syndrome?
``` o Keeping whole body warm (gloves/warm socks) o Smoking cessation o Regular exercise o Avoiding stress o Stop drug exacerbating Raynaud’s ```
126
Drug management of Raynaud's syndrome?
If lifestyle advice fails o Medication  Nifedipine 5mg TDS and titrate up to 20mg TDS o Refer if that fails
127
Complications of Raynaud's syndrome?
o Digital ischaemia o Gangrene o Digital Ulcers o Infection
128
Definition of lymphoedema?
- Atypical collection of lymph fluid within body tissues | - Due to failure to clear fluid and macromolecules by lymphatic system
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Types of lymphoedema?
o Primary lymphoedema – congenital insufficiency of lymphatic system  Milroy’s disease  Turner’s syndrome o Secondary lymphoedema – damage to lymphatic system or removal of lymph nodes by surgery/radiotherapy/infection or injury  Malignancy (most commonly arms in breast cancer) (or its treatments)  Recurrent lymphangitis (erysipelas, chronic venous ulceration)  Lymph obstruction (tumour, TB, filariasis)
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Causes of lymphoedema?
o Malignancy (or its treatment)
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Symptoms of lymphoedema?
``` o Progressive swollen, firm limbs  Arms and legs affected more often  Poorly pitting o Heaviness or fullness of limb o Tight sensation in skin ```
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Signs of lymphoedema?
o Kaposi-Stemmer sign – inability to pinch fold of skin on dorsal surface of foot at base of second toe o Poorly pitting oedema o Recurrent infections of limbs
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Diagnosis and investigations of lymphoedema?
- Clinical diagnosis - Lymphangosyntigraphy o Diagnostic - Lymphangiography o Shows lymph hypoplasia, hyperplasia or retrograde obliteration
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Management of lymphoedema - general advice?
o Skin and nail care – reduce infection risk o Elevation of limbs above level of heart when possible o Regular exercise
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Management of lymphoedema - conservative management?
o Compression stockings o Manual lymph drainage o Intermittent pneumatic compression
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Management of lymphoedema - surgical management?
o If non-surgical methods have failed | o Liposuction, debulking and bypass operations
Year 5 Core Conditions
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